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Results: 1 to 20 of 42

References for PMC Articles for PubMed (Select 18984148)

1.

Identifying autism loci and genes by tracing recent shared ancestry.

Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA.

Science. 2008 Jul 11;321(5886):218-23. doi: 10.1126/science.1157657. Erratum in: Science. 2010 Dec 24;330(6012):1746.

2.

Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo.

Li H, Radford JC, Ragusa MJ, Shea KL, McKercher SR, Zaremba JD, Soussou W, Nie Z, Kang YJ, Nakanishi N, Okamoto S, Roberts AJ, Schwarz JJ, Lipton SA.

Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9397-402. doi: 10.1073/pnas.0802876105. Epub 2008 Jul 1.

3.

Structural variation of chromosomes in autism spectrum disorder.

Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW.

Am J Hum Genet. 2008 Feb;82(2):477-88. doi: 10.1016/j.ajhg.2007.12.009. Epub 2008 Jan 17.

4.

Disruption of neurexin 1 associated with autism spectrum disorder.

Kim HG, Kishikawa S, Higgins AW, Seong IS, Donovan DJ, Shen Y, Lally E, Weiss LA, Najm J, Kutsche K, Descartes M, Holt L, Braddock S, Troxell R, Kaplan L, Volkmar F, Klin A, Tsatsanis K, Harris DJ, Noens I, Pauls DL, Daly MJ, MacDonald ME, Morton CC, Quade BJ, Gusella JF.

Am J Hum Genet. 2008 Jan;82(1):199-207. doi: 10.1016/j.ajhg.2007.09.011.

5.

Vasopressin: behavioral roles of an "original" neuropeptide.

Caldwell HK, Lee HJ, Macbeth AH, Young WS 3rd.

Prog Neurobiol. 2008 Jan;84(1):1-24. Epub 2007 Nov 4. Review.

6.

Contribution of SHANK3 mutations to autism spectrum disorder.

Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW.

Am J Hum Genet. 2007 Dec;81(6):1289-97. Epub 2007 Oct 16.

7.

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Kirov G, Gumus D, Chen W, Norton N, Georgieva L, Sari M, O'Donovan MC, Erdogan F, Owen MJ, Ropers HH, Ullmann R.

Hum Mol Genet. 2008 Feb 1;17(3):458-65. Epub 2007 Nov 6.

8.

Attachment, aggression and affiliation: the role of oxytocin in female social behavior.

Campbell A.

Biol Psychol. 2008 Jan;77(1):1-10. Epub 2007 Sep 6. Review.

PMID:
17931766
9.
10.

Abnormal social behaviors in mice lacking Fgf17.

Scearce-Levie K, Roberson ED, Gerstein H, Cholfin JA, Mandiyan VS, Shah NM, Rubenstein JL, Mucke L.

Genes Brain Behav. 2008 Apr;7(3):344-54. Epub 2007 Oct 1.

PMID:
17908176
11.

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.

Tabuchi K, Blundell J, Etherton MR, Hammer RE, Liu X, Powell CM, Südhof TC.

Science. 2007 Oct 5;318(5847):71-6. Epub 2007 Sep 6.

12.

Disruption of cerebral cortex MET signaling in autism spectrum disorder.

Campbell DB, D'Oronzio R, Garbett K, Ebert PJ, Mirnics K, Levitt P, Persico AM.

Ann Neurol. 2007 Sep;62(3):243-50.

PMID:
17696172
13.

Genomic rearrangements and sporadic disease.

Lupski JR.

Nat Genet. 2007 Jul;39(7 Suppl):S43-7. Review.

PMID:
17597781
14.

Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2.

Chubykin AA, Atasoy D, Etherton MR, Brose N, Kavalali ET, Gibson JR, Südhof TC.

Neuron. 2007 Jun 21;54(6):919-31.

15.

Localizing recent adaptive evolution in the human genome.

Williamson SH, Hubisz MJ, Clark AG, Payseur BA, Bustamante CD, Nielsen R.

PLoS Genet. 2007 Jun;3(6):e90. Epub 2007 Apr 20.

16.

Patterning of frontal cortex subdivisions by Fgf17.

Cholfin JA, Rubenstein JL.

Proc Natl Acad Sci U S A. 2007 May 1;104(18):7652-7. Epub 2007 Apr 18.

17.

Strong association of de novo copy number mutations with autism.

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimäki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M.

Science. 2007 Apr 20;316(5823):445-9. Epub 2007 Mar 15.

18.

Reversal of neurological defects in a mouse model of Rett syndrome.

Guy J, Gan J, Selfridge J, Cobb S, Bird A.

Science. 2007 Feb 23;315(5815):1143-7. Epub 2007 Feb 8.

19.

Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

Giacometti E, Luikenhuis S, Beard C, Jaenisch R.

Proc Natl Acad Sci U S A. 2007 Feb 6;104(6):1931-6. Epub 2007 Jan 31.

20.

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.

Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F, Nygren G, Rastam M, Gillberg IC, Anckarsäter H, Sponheim E, Goubran-Botros H, Delorme R, Chabane N, Mouren-Simeoni MC, de Mas P, Bieth E, Rogé B, Héron D, Burglen L, Gillberg C, Leboyer M, Bourgeron T.

Nat Genet. 2007 Jan;39(1):25-7. Epub 2006 Dec 17.

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